DRESSINgDACC Coated Post-operative Dressings for Surgical Site Infection Prevention in Vascular Surgery
This study aims to evaluate if DACC coated post-operative dressings can prevent surgical site infections within 30 days after vascular surgery.
DACC-Coated Post Operative Dressing
Surgical Wound+7
+ Bacterial Infections and Mycoses
+ Bacterial Infections
Treatment Study
Summary
Study start date: January 19, 2017
Actual date on which the first participant was enrolled.This study focuses on surgical site infections, which are infections that occur at the site of surgery and affect around 5% of people who undergo operations. The rate is even higher in vascular surgery, reaching up to 30%. The study aims to investigate the effectiveness and cost-effectiveness of a method to reduce these infection rates. The method involves using Leukomed Sorbact, a wound dressing coated with a chemical called Dialkylcarbamoylchloride (DACC). This chemical is derived from spider-silk and interacts with bacteria, causing them to be removed from the wound when the dressing is changed. The study targets adults undergoing vascular surgery, a population that is particularly at risk of surgical site infections. In this study, 718 patients from various centers across the UK will participate. They will be randomly assigned by computer to one of two groups. One group will have their wounds dressed with Leukomed Sorbact, while the other group will receive a standard dressing. The study will follow up with the patients 30 days after their operation to inspect their wounds for infection. Patients will also be asked to complete short questionnaires about their quality of life at this time and again at 3 months post-surgery. The main question the study aims to answer is whether a DACC-coated dressing applied after an operation reduces the risk of infection at the surgery site. The study will also explore whether this treatment is cost-effective and promotes satisfactory healing.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.722 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal Infirmary
Hull, United KingdomOpen Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal Infirmary in Google Maps